Quality control Work, Jobs in Aldermaston, Brk (with Salaries)

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
4d
Quality Inspector
FOX-VPS Ltd —Camberley
- From £36,000 a year
- Full-time
- Organisational skills
- In-person
- Communication skills
Quick apply
6d
Quality Control Chemist
Biosynth Carbosynth —Newbury
- £28,000 - £29,000 a year
- Full-time
- Computer literacy
- Laboratory experience
- Bachelor's degree
- Free parking
- Sick pay
Quick apply
2d
Quality Assurance Engineer
Chroma Engineering —Didcot
- £45,000 - £65,000 a year
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
- Referral programme
Quick apply
12d
Quality Control Inspector
Jabil Circuit —Thatcham
- Full-time
- Microsoft Excel
- Microsoft Office
- Computer skills
13d
Quality Control Process Technician
Elements Solutions Inc —Wantage
- Microsoft Excel
- Quality control
- IT
- Free parking
Head, PV and Regulatory QA
CSL Seqirus —Maidenhead
- Full-time
- Customer service
- Bachelor's degree
- Organisational skills
Quality Inspector
AWE —Reading
- From £39,280 a year
- Full-time
- In-person
- Free parking
- Annual leave
Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Analysis skills
- Work from home
6d
Quality, Goods In & Stock Controller
Summit Oxygen —Hartley Wintney
- £27,000 - £30,000 a year
- Full-time
- English
- Assembly
- Organisational skills
- Free parking
- Annual leave
Quick apply
Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
6d
Quality Assurance Engineer
MDA Space —Didcot
- Hybrid work
- Engineering
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Life insurance
Quality Engineer (Medical Devices)
Amber Therapeutics —Didcot
- Full-time
- Hybrid work
- Engineering
- Quality control
- Communication skills
Quick apply
Quality Assurance Officer II
Replimune —Abingdon
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
6d
Quality Assurance Officer I
Replimune —Abingdon
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
5d
Quality Assurance Engineer
MDA —Didcot
- Full-time
- Hybrid work
- Engineering
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Life insurance
Quality Control (QC) Engineer (shift based)
Open Cosmos —Didcot
- Rotating shift
- English
Quality Inspector - Aerospace/Space
TISICS —Farnborough
- Communication skills
Quality Manager – Asbestos (6 month fixed term contract)
Tetra tech Ltd. —Basingstoke
- Continuous improvement
- In-person
Quick apply
Quality System Specialist
Loftware, Inc. —Reading
- Hybrid work
- English
- Quality control
- Organisational skills
Quick apply

I want to receive the latest job alerts for quality control in aldermaston, brk

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

quality control jobs near aldermaston, brk

Compliance Officer jobs in Reading

Structural Engineer jobs in London

Live Sound Engineer jobs in London

Quality Assurance Engineer jobs in Lydd

Quality Assurance Engineer jobs in Telford

Quality Assurance Engineer jobs in Sheffield

Electrical Design Engineer jobs in London

Quality Control Associate jobs in Armthorpe

Quality Control Associate jobs in Cheadle Hulme

Physician Associate jobs in Birmingham

Quality Manager jobs in Bristol

Associate Structural Engineer jobs in London

Quality Assurance Engineer jobs in Sittingbourne

Quality Assurance Engineer jobs in London

Artificial Intelligence Engineer jobs in England

Quality Assurance Engineer jobs in Liverpool

Software Engineer jobs in Edinburgh

Quality Assurance Engineer jobs in Westhill And District

Senior Quality Assurance Specialist jobs in Swindon

Senior Quality Assurance Specialist jobs in Macclesfield

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

IQVIA -
Reading

Apply Now

Job details

Full-time
4 days ago

Benefits

UK visa sponsorship
Work from home

Qualifications

Clinical research
English
Microsoft Office
Bachelor's degree
Continuous improvement
Organisational skills
Computer skills
Root cause analysis
Leadership
Communication skills
Negotiation

Full job description

Reading, United Kingdom | Full time | Home-based | R1559367

General Description:

The Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effective inspection readiness programs, and successful management of inspections and audits.

Key responsibilities include leading inspection readiness and audit support activities at regional or global levels, guiding clinical teams on inspection expectations, coordinating audit and inspection responses, and ensuring timely, high-quality, and compliant remediation. The role also drives a proactive inspection/audit readiness culture, to effectively manage complex, high-risk inspections while maintaining continuous readiness.

Inspection readiness implementation and oversight
• Organize briefing materials, logistics, and stakeholder alignment
• Support inspection readiness across the EMEA region
• Support implementation of standards, tools, and best practices
• Ensure teams are inspection-ready through training and guidance
• Assess inspection risks and oversee mitigation plans
• Supports mock inspections and readiness assessments
• Maintain inspection-ready documentation, processes, and systems
• Supports development of story boards based on global story boards templates and structure and acting as subject matter expert (SME) in content generation together with the relevant functional area SMEs

Inspection and Audit Preparation, Execution and Follow up
• Support regional preparation activities for regulatory inspections and internal/external audits
• Coordinate cross-functional stakeholders (Clinical Operations, QA, country teams)
• Align with Regional Clinical Compliance Lead to conduct targeted site preparation visits as required

Post-Inspection/Audit Activities
• Lead and coordinate responses to inspection/audit findings
• Manage CAPAs, including risk assessment, root cause analysis, and effectiveness checks
• Track CAPAs to timely and effective closure
• Ensure robust root cause analysis and sustainable corrective actions
• Oversee CAPA strategies and regulatory commitments
• Drive consistent, high-quality organizational responses
• Monitor trends and identify opportunities for continuous improvement

Core Competencies, Knowledge and Skill Requirements:

• Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated regulatory guidelines
• Analytical and problem-solving skills and high attention to detail, and quality orientation
• Excellent communication and stakeholder management skills
• Influence senior stakeholders and decision-making

Communication & Interpersonal Skills:
• Excellent English written and verbal communication and interpersonal skills
• Excellent organizational skills and ability to prioritize and multi-task
• Ability to work independently in multi-cultural setting and effectively handle multiple priorities in a fast-paced environment

Qualifications
Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with 10+ years in clinical research, clinical operations, or compliance.
Minimum 4 years’** experience in a GCP compliance or equivalent role* (i.e. quality) is preferred.

• Experience in CAPA development and tracking
• Experience in inspections and audits management, including mock inspections and mock interviews
• Deep knowledge of ICH-GCP, regulatory requirements and Clinical trial processes end-to-end
• Experience in oncology global trials is preferred
• Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
• Sound working knowledge of relevant terminology, International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), applicable regulatory requirements, quality management processes.
• Excellent organizational, interpersonal and communication skills.
• Excellent judgement and decision-making skills.
• Demonstrated leadership and line management skills.
• Excellent influencing and negotiation skills.
• Strong computer skills including Microsoft Office applications.
• Excellent problem-solving skills.
• Demonstrated ability to work in a matrix environment.
• Ability to lead and motivate a clinical team also required.
• Ability to travel within the region/country.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Fluent in English.

Please note: this role is not eligible for the UK VISA sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

quality control jobs in aldermaston, brk

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Quality Inspector

Quality Control Chemist

Quality Assurance Engineer

Quality Control Inspector

Quality Control Process Technician

Head, PV and Regulatory QA

Quality Inspector

Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead

Quality, Goods In & Stock Controller

Quality Associate II, Quality Assurance

Quality Assurance Engineer

Quality Engineer (Medical Devices)

Quality Assurance Officer II

Quality Assurance Officer I

Quality Assurance Engineer

Quality Control (QC) Engineer (shift based)

Quality Inspector - Aerospace/Space

Quality Manager – Asbestos (6 month fixed term contract)

Quality System Specialist

I want to receive the latest job alerts for quality control in aldermaston, brk

Explore jobs in more locations

Where you'll work

Home-based

Culture

Jobseeker tools

Employer Tools

Browse

Stay Connected